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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118131Generated: October 31, 2026

Methanesulfonyl chloride → HCID 11317958, compound

https://huagongshe.com/reaction/2118131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 69227813HCID 69227813—
ProductHCID 11317958HCID 11317958—

Reaction Steps

The title compound was prepared from ethyl 5-amino-1-benzhydryl-3-phenyl-1H-indole-2-carboxylate and methanesulfonyl chloride followed the procedure of Example 1 Step 3 as an off-white solid: 1H NMR (DMSO-d6) δ 2.85 (s, 3H, 6.79 (d, J=9.0 Hz, 1H, 6.95 (dd, J=9.0, 2.0 Hz, 1H, 7.19 (d, J=7.4 Hz, 4H, 7.30-7.50 (m, 12H, 7.91 (s, 1H, 9.37 (s, 1H, 13.21 (br s, 1H; MS (ESI) m/z 495 [M-H]−; HRMS calcd for C29H25N2O4S: 497.1533; found (ESI+): 497.1522; Anal. calcd for C29H24N2O4S.0.7H2O: C, 68.41; H, 5.03; N, 5.50. Found: C, 68.32; H, 4.91; N, 5.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442805B2
Source datasetuspto-grants-2008_10
ORD IDord-561ad9d8698d40789df1dba30c66628d
Source noteuspto-grants-2008_10