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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768496Generated: November 2, 2026

HCID 9805055, compound → HCID 10939534, compound

https://huagongshe.com/reaction/1768496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 9805055HCID 9805055—
ReactantHCID 9847903HCID 9847903—
ReactantHCID 9912250HCID 9912250—
ReactantHCID 9912251HCID 9912251—
ReactantHCID 9934122HCID 9934122—
ReactantHCID 10885254HCID 10885254—
ReactantHCID 11134719HCID 11134719—
SolventMethanolHCID 887—
ProductHCID 10939534HCID 10939534—

Reaction Steps

colorless amorphous solid; [α]22D −84 (c 0.2, MeOH); UV (MeOH) λmax nm (ε) 211 (17400), 248 (12900); 1R (KBr) νmax 3433, 2961, 2933, 2879, 1730, 1708, 1457, 1251, 975 cm−1; 1H NMR (CDCl3, 600 MHz) δ 7.00 (1H, s, H-19),6.64 (1H, bs H17),5.45 (1H, ddd, J=15.2, 6.5, 6.5 Hz, H-12),5.42 (1H, dd, J=6.4, 3.7 Hz, H-15),5.35 (1H, dt, J=15.2, 7.1 Hz, H-13), 4.42 (1H, m, H-3),3.58 (1H, ddd, J=8.1, 7.9, 2.8 Hz, H-7),3.24 (1H, m, H-6), 3.14 (1H, dq, J=4.0, 6.9 Hz, H-6), 2.92 (1H, d, J=7.9 Hz, 7-OH), 2.71 (3H, s, H-21), 2.71 (2H, m, H-2), 2.53 (2H, m, H-14), 2.17 (1H, d, J=2.17 Hz, 3-OH), 2.11 (1H, m, H-11a), 2.06 (3H, bs, H-27), 1.93 (1H, m, H-11b), 1.68 (1H, m, H-9a), 1.65 (1H, m, H-10a), 1.33 (1H, m, H-8), 1.26 (3H, d, J=6.8 Hz, H-24), 1.16 (1H, m, H-10b), 1.12(3K d, J=6.9 Hz, H-22), 1.07 (1H, m, H-9b), 1.00 (3H, d, J=6.8 Hz, H-25); 13C NMR, see Table 1; EIMS m/z 463 [M]+ (6),290 (21), 289 (20), 204 (23), 194 (19), 190 (22), 168 (100), 164 (48), 157 (14), 152 (19), 151 (17), 139 (15), 111 (18); HREIMS m/z 463.2371 (calcd. for C25H37NO5S, 463.2392).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235669B2
Source datasetuspto-grants-2007_06
ORD IDord-af75b1c65ccd476fb0c29cbe0c097bcf
Source noteuspto-grants-2007_06