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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879510Generated: October 31, 2026

HCID 86700328, compound → HCID 86700332, compound

https://huagongshe.com/reaction/879510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86700328HCID 86700328—
ReactantHCID 86700330HCID 86700330—
ProductHCID 86700332HCID 86700332—

Reaction Steps

(2S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(4-methyl-3-(1-methyl-1H-indazol-5-yl)piperazin-1-yl)benzo[d]thiazol-6-yl)acetic acid (12 mg) was prepared in a similar manner as compound (2S)-2-tert-butoxy-2-(2-(4-(tert-butoxycarbonyl)-3-(1-methyl-1H-indazol-5-yl)piperazin-1-yl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)acetic acid except using (2S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(4-methyl-3-(1-methyl-1H-indazol-5-yl)piperazin-1-yl)benzo[d]thiazol-6-yl)acetate instead of tert-butyl 4-(6-((S)-1-tert-butoxy-2-ethoxy-2-oxoethyl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-2-yl)-2-(1-methyl-1H-indazol-5-yl)piperazine-1-carboxylate. LCMS-ESI+: calc'd for C33H37ClN5O3S: 618.2 (M+H+); Found: 618.4 (M+H+). 1H-NMR 400 MHz, (CD3OD) δ 8.11 (m, 1H), 7.98 (m, 1H), 7.77 (m, 1H), 7.60 (m, 1H), 7.55-7.46 (m, 4H), 7.38 (s, 1H), 5.15 (s, 1H), 4.40 (m, 2H), 4.35 (m, 1H), 4.11 (s, 3H), 3.9-3.7 (m, 3H), 3.45 (m, 1H), 2.68 (s, 3H), 2.50 (s, 3H), 0.94 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-bdbb4dac8ab44c3986d6c73c87f032f4
Source noteuspto-grants-2015_03