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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794735Generated: November 3, 2026

Acetic Acid → HCID 10168421, compound

https://huagongshe.com/reaction/1794735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
ReactantHCID 22220437HCID 22220437—
SolventDimethylformamideHCID 6228—
ProductHCID 10168421HCID 1016842168.5%

Reaction Steps

Acetic acid (0.12 mL, 2.16 mmol) was added to a mixture of N-{5-[(1R)-2-amino-1-hydroxyethyl]-2-hydroxyphenyl}methanesulfonamide (266 mg, 1.08 mmol) (which was obtained in Example 10), tert-butyl 2-{2,4-dioxo-5-[4-(4-oxo-1-piperidinyl)benzyl]-1,3-thiazolidin-3-yl}acetate (450 mg, 1.08 mmol) (which was obtained in Example 49), and DMF (5 mL). The mixture was stirred for 20 minutes and then, sodium triacetoxyborohydride (276 mg, 1.3 mmol) was added, and the new mixture was stirred at room temperature for 24 hours. The volatiles were removed in vacuo and the residue was purified by flash chromatography (dichloromethane/methyl alcohol 5/1) to produce a yellow solid (480 mg, 68% yield); mp 130–132° C.; 1H NMR (400 MHz, DMSO-d6) δ 1.20–1.50 (m, 11 H), 1.81–1.85 (m, 2H), 2.60–2.80 (m, 4H), 2.85–2.9 (m, 4H), 3.40 (m, 1H), 3.60 (m, 1H), 4.20 (s, 2H), 4.50 (m, 1H), 5.04 (m, 1H), 6.80–6.87 (m, 3H), 7.02 (m, 1H), 7.08 (m, 2H), 7.20 (m, 1H); Anal. Calcd. for C30H40N4O8S2: C, 55.54; H; 6.21; N, 8.64. Found: C, 53.86; H, 6.11; N, 7.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022716B2
Source datasetuspto-grants-2006_04
ORD IDord-d74363e2a9d84d4395f14b7b2fe7aae2
Source noteuspto-grants-2006_04